Evidence map›Paper›PMID 36914891›Full record

ArticleNature immunology2023

A single-amino acid substitution in the adaptor LAT accelerates TCR proofreading kinetics and alters T-cell selection, maintenance and function.

Wan-Lin Lo, Miriam Kuhlmann, Gabrielle Rizzuto, H Atakan Ekiz, Elizabeth M Kolawole, Monica P Revelo, Rakieb Andargachew, Zhongmei Li, Yuan-Li Tsai, Alexander Marson and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Nature immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.3field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 32 citations in OpenAlex.

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  12. Proofreading and single-molecule sensitivity in T cell receptor signaling by condensate nucleation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Review
  14. Article
  15. ImmunOctoberfest reloaded.Nature immunology · 2025
    Article
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  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 3 countries.

Wan-Lin LoDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA. wan-lin.lo@path.utah.edu.ORCID 0000-0002-9074-6847
Miriam KuhlmannDivision of Animal Physiology and Immunology, School of Life Sciences, Technical University of Munich, Freising, Germany.ORCID 0000-0001-7431-9637
Gabrielle RizzutoHuman Oncology and Pathogenesis Program, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0003-3052-0253
H Atakan EkizDepartment of Molecular Biology and Genetics, Izmir Institute of Technology, Gulbahce, Turkey.
Elizabeth M KolawoleDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID 0000-0003-3138-0037
Monica P ReveloDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Rakieb AndargachewDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Zhongmei LiDepartment of Microbiology and Immunology, University of California San Francisco, San Francisco, CA, USA.
Yuan-Li TsaiDivision of Rheumatology, Rosalind Russell and Ephraim P. Engleman Arthritis Research Center, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.
Alexander MarsonDepartment of Microbiology and Immunology, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-2734-5776
Brian D EvavoldDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Dietmar ZehnDivision of Animal Physiology and Immunology, School of Life Sciences, Technical University of Munich, Freising, Germany. dietmar.zehn@tum.de.ORCID 0000-0003-1393-8527
Arthur WeissDivision of Rheumatology, Rosalind Russell and Ephraim P. Engleman Arthritis Research Center, Department of Medicine, University of California San Francisco, San Francisco, CA, USA. arthur.weiss@ucsf.edu.ORCID 0000-0002-2414-9024
University of Utah · USUniversity of California, San Francisco · USTechnical University of Munich · DEGladstone Institutes · USIzmir Institute of Technology · TRMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Understand the metabolic fitness of naïve T cellsP01AI091580 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JEROEN ROOSE · 2011 to 2026
$31.1M
Molecular and Cellular Mechanisms in CancerT32CA108462 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GOGA, ANDREI · 2004 to 2024
$10.4M
CD8 T cell antigen recognition during chronic infectionR01AI147641 · NIAID · UNIVERSITY OF UTAH · PI EVAVOLD, BRIAN D · 2020 to 2024
$3.3M
Pathogenic low affinity CD8 T cells in malariaR01AI167422 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI EVAVOLD, BRIAN D, LAMB, TRACEY JANE · 2021 to 2025
$3.3M
Maternal T cell recognition of placental antigenK08AI137209 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RIZZUTO, GABRIELLE A · 2018 to 2022
$1.0M
Regulation of T cell ligand discrimination by tuning the phosphorylation kinetics of Zap70 substratesK22AI143960 · NIAID · UNIVERSITY OF UTAH · PI LO, WAN-LIN · 2021 to 2022
$270k
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA108462NIAID NIH HHS K08 AI137209NIAID NIH HHS K22 AI143960NIAID NIH HHS P01 AI091580NIAID NIH HHS R01 AI147641NIAID NIH HHS R01 AI167422
6 · The paper itself

Abstract

Mature T cells must discriminate between brief interactions with self-peptides and prolonged binding to agonists. The kinetic proofreading model posits that certain T-cell antigen receptor signaling nodes serve as molecular timers to facilitate such discrimination. However, the physiological significance of this regulatory mechanism and the pathological consequences of disrupting it are unknown. Here we report that accelerating the normally slow phosphorylation of the linker for activation of T cells (LAT) residue Y136 by introducing an adjacent Gly135Asp alteration (LAT

Indexed as

Adaptor Proteins, Signal TransducingT-LymphocytesAmino Acid SubstitutionAnimalsLymphocyte ActivationMicePhosphoproteinsPhosphorylationReceptors, Antigen, T-CellAdaptor Proteins, Signal TransducingPhosphoproteinsReceptors, Antigen, T-Cell

Identifiers

PMID36914891
PMCPMC10063449
OpenAlexW4324044817

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.